Gene dose-dependent control of hematopoiesis and hematologic tumor suppression by CBP

Mice with monoallelic inactivation of the CBP gene develop highly penetrant , multilineage defects in hematopoietic differentiation and, with advancing age, an increased incidence of hematologic malignancies. The latter are ch aracterized, at least in some cases, by loss of heterozygosity (LOH) at the CBP locus. No such pathology was observed in wild-type or p300 heterozygou s null mice of the same age and genetic background. Thus, a full complement of CBP, but not p300, is required for normal hematopoietic differentiation . These results also provide the first experimental evidence for the hypoth esis that CBP has tumor-suppressing activity.